Highly selective and efficient ammonia synthesis from N2 and H2O via an iron-based electrolytic-chemical cycle

被引:22
作者
Cui, Baochen [1 ,2 ]
Yu, Zhongjun [2 ]
Liu, Shuzhi [1 ,2 ]
Zhang, Jianhua [2 ]
Liu, Xianjun [2 ]
Liu, Chang [2 ]
Zhang, Zhihua [1 ]
机构
[1] Guangdong Univ Petrochem Technol, Sch Chem Engn, Maoming 525000, Peoples R China
[2] Northeast Petr Univ, Coll Chem & Chem Engn, Prov Key Lab Oil & Nat Gas Chem Ind, Daqing 163318, Peoples R China
关键词
Ammonia synthesis; Electrolytic-chemical cycle; Fe2O3/AC; Molten hydroxide electrolyte; ELECTROCHEMICAL SYNTHESIS; ATMOSPHERIC-PRESSURE; WET AIR; REDUCTION; FIXATION; NITROGEN; METAL; ELECTROCATALYST; TEMPERATURE; COMPOSITE;
D O I
10.1016/j.ijhydene.2019.10.144
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Ammonia production via electroreduction of N-2 and water under mild conditions is emerging as a promising alternative to the fossil fuels-reliance and CO2 emitting Haber-Bosch process. However, the achievement of high Faradaic efficiency and high ammonia formation rate is still challenging. Here, we demonstrate how ammonia can be selectively produced from N-2 and H2O via a two-step iron-based cyclic process using a molten hydroxide electrolyte. The first step is the production of Fe by electrochemical reduction of Fe2O3. The second step is the steam-hydrolysis of Fe with bubbling N-2 to produce NH3 and reform Fe2O3. Both reaction steps proceed isothermally at 250 degrees C in a molten salt electrolytic cell without switching of temperature and needing separation of the mediator, resulting in more easily putting into industrial practice. The cycle achieves an ultrahigh Faradaic efficiency of 79.8% at 1.15 V and a high ammonia formation rate of 1.34 x 10(-8) mol s(-1) cm(-2) at 1.75 V. This is a critical advance in breaking the domination of hydrogen evolution reaction (HER) competition to achieve highly selective and efficient NH3 synthesis from N-2 and H2O beyond reliance of fossil fuels. (C) 2019 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:94 / 102
页数:9
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